Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 69038-74-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
tert-Butyl 3-bromobenzoate features a brominated aromatic ring coupled with a sterically hindered tert-butyl ester, enabling robust stability and compatibility in cross-coupling reactions. This combination facilitates efficient C–C bond formation under standard conditions, delivering high functional group tolerance and predictable regiochemistry.
tert-Butyl 3-Bromobenzoate serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions such as Suzuki and Stille couplings. The bromo group provides high reactivity under standard conditions, while the tert-butyl ester offers excellent bench stability and facile deprotection via mild acidic conditions. Its functional group tolerance and predictable reactivity make it ideal for constructing complex aromatic scaffolds in medicinal chemistry and materials science applications.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: